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Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.
for Ethyl Acetate/Water [3] P = 760 mmHg BP Temp. °C % by mole C 4 H 8 O 2; liquid vapor 100.0: 0.0: ... (in ethyl), 7.1 Hz. MS; Masses of main fragments 88.0 (5.1% ...
For esters such as ethyl acetate (CH 3 COOCH 2 CH 3), ethyl formate (HCOOCH 2 CH 3) or dimethyl phthalate that are based on common acids, IUPAC recommends use of these established names, called retained names. The "-oate" changes to "-ate." Some simple examples, named both ways, are shown in the figure above.
n.o.s. = not otherwise specified meaning a collective entry to which substances, mixtures, solutions or articles may be assigned if a) they are not mentioned by name in 3.2 Dangerous Goods List AND b) they exhibit chemical, physical and/or dangerous properties corresponding to the Class, classification code, packing group and the name and description of the n.o.s. entry [2]
An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).
(CH 3) 2 SO 189 °C 46.7 1.10 g/cm 3: 3.96 reacts with strong bases, difficult to purify ethyl acetate: C 2 H 5 OCOCH 3: 77.1°C 6.02 0.902 g/cm 3: 1.88 reacts with strong bases hexamethylphosphoramide [(CH 3) 2 N] 3 PO 232.5 °C 29.6 1.03 g/cm 3: 5.38 high boiling point, high toxicity propylene carbonate: CH 3 C 2 H 3 O 2 CO 242 °C 64.9 1.205 ...
C 4 H 7 NO 2: 1-Aminocyclopropanecarboxylic acid: 22059-21-8 C 4 H 7 NO 3: aceturic acid: C 4 H 7 NO 4: aspartic acid Asp: 56-84-8 C 4 H 8: cyclobutane: 287-23-0 C 4 H 8 N 2 O 3: asparagine Asn: 70-47-3 C 4 H 8 O: tetrahydrofuran THF: 109-99-9 C 4 H 8 O 2: ethyl acetate: C 4 H 8 O 3: gamma-Hydroxybutyric acid: 591-81-1 C 4 H 9 ClHg n ...
acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...